Special

HsaINT0044336 @ hg38

Intron Retention

Gene
ENSG00000073067 | CYP2W1
Description
cytochrome P450 family 2 subfamily W member 1 [Source:HGNC Symbol;Acc:HGNC:20243]
Coordinates
chr7:984412-985099:+
Coord C1 exon
chr7:984412-984574
Coord A exon
chr7:984575-984949
Coord C2 exon
chr7:984950-985099
Length
375 bp
Sequences
Splice sites
5' ss Seq
GAGGTCGGT
5' ss Score
5.44
3' ss Seq
CGCACTGTATCTGCCTACAGGCA
3' ss Score
8.73
Exon sequences
Seq C1 exon
CTCTCAGAACGCTACGGGCCGGTGTTCACCGTGCACCTGGGGCGCCAGAAGACGGTGGTGCTGACGGGGTTCGAGGCGGTCAAAGAGGCGCTGGCGGGCCCCGGGCAGGAGCTGGCCGACCGGCCTCCCATCGCCATCTTCCAGCTCATCCAGCGAGGTGGAG
Seq A exon
GTCGGTGTGTGGCCGGCGCTACGGGGCCTACTGGGTGTGGGGGCACCTGGACCCCAGGAGGGGTGGGGGCTCCAGCAGCGGGAGAGGCTCCCAGGGTGGCCTGGGGAAGAGCAGGCAGGAGCTGGGCCTCCGGGCTGGTGCTGAGAAGGGCCAGGTGTCCACACAGCAGGTCAGGTGCTCAGAACCAGCAAGCGGGGTTCTTTTCATCCCAAGTCAAGAGGGGCCAGGGCCAGCCCAGGGGGACGGGAGTGGGGATGGGGGTGAGGGCCCAGCCAGTCTCGCTGCCCTGTCAGCCTGCTCACTTCCTGCCCACTTGCCTGGCGGGGCTGGCTGGGGTGGGAACCTGGGCTCACCACGCACTGTATCTGCCTACAG
Seq C2 exon
GCATCTTCTTCTCATCTGGGGCGCGCTGGAGGGCTGCCCGCCAGTTCACGGTGCGTGCCCTGCACAGCCTGGGCGTGGGCCGGGAGCCGGTGGCTGACAAGATTCTGCAGGAGCTGAAATGCCTCTCTGGGCAGCTGGATGGCTACAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000073067:ENST00000308919:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0006717=p450=FE(11.9=100)
A:
NA
C2:
PF0006717=p450=FE(11.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTCTCAGAACGCTACGGGCC
R:
CTCTGTAGCCATCCAGCTGC
Band lengths:
313-688
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development